A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149936



Internal ID20716976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114969243..114969759hg38UCSC Ensembl
chr7:114609298..114609814hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606947
Supporting Variants
Samples
Known GenesMDFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00094


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